Clinical Research Regulatory Specialist

• Bachelor's degree in life sciences, clinical research, or a related field.
• 1-2 years of clinical trial experience; regulatory experience preferred.
• Working knowledge of GCP and IRB processes; familiarity with FDA regulations and 21 CFR Part 11 preferred.
• Experience with eReg or eSource systems preferred (CRIO a plus).
• Strong written and verbal communication skills with PIs, sponsors, CROs, and site teams.
• Collaborative and respectful, with a kind, patient approach to working with site staff and colleagues, including under tight deadlines.
• Results-driven, taking ownership, following through, and adapting as priorities shift.
• Detail-oriented and thorough, catching discrepancies such as outdated ICF versions and confirming documents are filed and communicated to the right people.

Pay: $60-75k salary, commensurate with experience